ライフサイエンスコーパス: homo-

1 ving rise to an elongated C-C bond or "super-HOMO".

2 l as the highest occupied molecular orbital (HOMO).

3 correlated with the bridge barrier E(F) - E(HOMO).

4 2D/G12D bone marrow cells develop TALL (TALL-homo).

5 s determined by the bridge barrier, E(F) - E(HOMO).

6 tes and other reaction parameters and permit homo- ((1)H-(1)H) and heteronuclear ((1)H-(13)C) 2D NMR

7 The resulting trishomocyclopropyl HOMO{-1} is a three-center two-electron bond responsible

8 e C1, C1', and C2' atoms is prominent in the HOMO{-1}.

9 LG), Ethiopia, place the first occurrence of Homo ~250 thousand years earlier than the Oldowan at Gon

10 y higher highest occupied molecular orbital (HOMO) (-5.43 eV) and lowest unoccupied molecular orbital

11 (-3.80 eV) energy levels relative to ITIC1 (HOMO: -5.48 eV; LUMO: -3.84 eV), and higher electron mob

12 These associate in vivo to form homo- (alpha(2)) and heterodimers (alpha.beta) with litt

13 both the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of

14 ween the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO)

15 ween the highest-occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO)

16 ween the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO)

17 and frontier orbitals of the aromatic donor (HOMO) and the NO(+) acceptor (LUMO) clearly suggests an

18 nid distinct from Pongo, Gigantopithecus and Homo, and further reveal that Dubois's H. erectus paraty

19 d to later hominins such as Paranthropus and Homo, and has implications for key morphological and beh

20 pecialization from Australopithecus to early Homo, and increasing dispersion in microwear complexity

21 eems to have varied little through the genus Homo, and it should not be used to account for other asp

22 met Neandertals, Denisovans, mid-Pleistocene Homo, and possibly H. floresiensis, with some degree of

23 ve a considerably deep ancestry in the genus Homo, and that the cranial morphology of Neanderthals re

24 In this study, the self-assembly of homo- and blended conjugated polymers which are confined

25 e mobility along vertical direction for both homo- and blended conjugated polymers.

26 Several lines of evidence from both homo- and block copolymerization results have demonstrat

27 or styrenic monomers during the synthesis of homo- and block copolymers as the stability and reactivi

28 applications of synthetic stimuli-responsive homo- and block polypeptides are reviewed.

29 ibuted to varying ionization efficiencies of homo- and copolyesters.

30 nces, and architectures of a wide variety of homo- and copolymeric materials, including multicomponen

31 into the ROMP mechanism, monomer design, and homo- and copolymerization rate trends offer a general s

32 reactivity relationships for stereoselective homo- and copolymerization.

33 tructure and sequence elucidation of complex homo- and copolymers is key for further understanding po

34 erous strategies have been developed for the homo- and cross coupling of alkynes to enynes via transi

35 The role of gold as the organizing metal in homo- and cross-coupling reactions is explored in this p

36 this contribution, poly(dimethylacrylamide) homo- and dimethylacrylamide/4-acryloylmorpholine block

37 ered radicals explains the lack of undesired homo- and direct coupling products (Ar-Ar, Ar-Alk) in th

38 on including inactivation of HK activity via homo- and hetero oligomerization, and cross-phosphorylat

39 only allows the production of angstrom-sized homo- and hetero-crystals, but also provides new experim

40 Both homo- and hetero-dimerization of BRAF and CRAF can modul

41 Competitive homo- and hetero-dimerization of their amino-terminal do

42 he CRISPR target region is PCR amplified and homo- and hetero-duplexed amplicons formed during the la

43 The encoded proteins form multiple homo- and hetero-interactions and localize within secret

44 g atomically precise materials with tailored homo- and hetero-interfaces, which can form functional h

45 s, photocatalysts and reusable scaffolds for homo- and hetero-intermolecular [2+2] photocycloaddition

46 interactions of murine GBPs (mGBP1/2/3/5/6), homo- and hetero-multimerization properties of mGBP2 and

47 o access a library of densely functionalized homo- and hetero-multivalent glycomimetics comprising al

48 All of these homo- and hetero-NCDs could be successively formed by se

49 stions on the functional differences between homo- and hetero-oligomeric AAA proteases.

50 istributive, leading to the synthesis of DNA homo- and hetero-oligomeric and -polymeric ladders rangi

51 in 1 (RHL1) and RHL2] can assemble into both homo- and hetero-oligomeric complexes, displaying three

52 FHR1, FHR2, and FHR5 circulate in plasma as homo- and hetero-oligomeric complexes, the formation of

53 and recognition, conformational changes, and homo- and hetero-oligomeric interactions within the supr

54 Using this pair, we measure homo- and hetero-oligomerization interactions in living

55 the pentraxin domain that is involved in the homo- and hetero-oligomerization of NPTX2 and NPTXR.

56 mical studies suggest formation of flotillin homo- and hetero-oligomers in other cell types, but so f

57 All AtHIR proteins could form homo- and hetero-oligomers in vivo and were enriched in

58 e oligomer stability and FRET efficiency for homo- and hetero-oligomers of fluorescent protein-labele

59 ce showing that IFITM family members work as homo- and hetero-oligomers to modulate virus entry.

60 ar-atomic resolution provides a template for homo- and hetero-PYD/PYD associations, as confirmed by s

61 RHA) showed aggregation enhancement for both homo- and hetero-systems, in presence of divalent Ca(2+)

62 There are homo- and hetero-trimeric types of collagen consisting o

63 ing strategy for the synthesis of oligomeric homo- and hetero[n]rotaxanes with precise control over t

64 analyses, we could assess the extent of both homo- and heteroagglomeration as well as particle sedime

65 Over time, CeO2-NPs tend to homo- and heteroaggregate and to accumulate on the surfi

66 n chemistry that determines NPs dissolution, homo- and heteroaggregation, and co- and competitive-ret

67 o-biaryl substituted alkynes into polycyclic homo- and heteroarenes of different size, shape, and cur

68 These include homo- and heteroarenes, rings of five to six atoms, and

69 ntroduced that enables the isolation of both homo- and heterobimetallic complexes of divalent first-r

70 ks have motivated the synthesis and study of homo- and heterobinuclear conjugates as light-harvesting

71 and excited-state features of many of these homo- and heterobinuclear phthalocyanine and/or porphyri

72 preparation of covalent and supramolecular, homo- and heterobinuclear systems based on phthalocyanin

73 ists to target these receptor complexes with homo- and heterobivalent ligands.

74 mum at 420 nm that is very different for the homo- and heterochiral diastereomers and of the concentr

75 PMD1 and PMD2 can form homo- and heterocomplexes.

76 Halogenated homo- and heterocyclic aromatics including disinfectants

77 etraspanins can physically interact, forming homo- and heterodimer complexes.

78 Moreover, they suggest that homo- and heterodimer formation poise C/EBPbeta to execu

79 with lapatinib and trastuzumab to block all homo- and heterodimer signaling as well as by blockade o

80 omers (2R,7R)- and (2S,7S)-2 and a series of homo- and heterodimeric analogues in which octanedioic a

81 epping kinetics of KIF3A and KIF3C motors in homo- and heterodimeric constructs and determine their t

82 y, the contrast between the functions of the homo- and heterodimeric forms of proteins deserves the a

83 Interestingly, the role of ABCD2 (in homo- and heterodimeric forms) in the metabolism of poly

84 tokine signaling induced by nonphysiological homo- and heterodimeric GFP-mCherry ligands.

85 A second domain, capable of mediating homo- and heterodimeric interactions between JPH1 and JP

86 esults suggest that the ability to establish homo- and heterodimeric interactions with resident JPHs

87 IM) domains (PAS-A and PAS-B), which mediate homo- and heterodimeric mPER-mPER interactions as well a

88 erbB3 homo- and heterodimerization events were captured in rea

89 mobilis TMY1009, rationalizing LsdA and LsdB homo- and heterodimerization in vivo A structure of an L

90 rted here reveal the molecular basis for the homo- and heterodimerization of AFF proteins and implica

91 Recent development suggests that homo- and heterodimerization of APP and APP-like protein

92 e is general and can be applied to study the homo- and heterodimerization of GPCRs and other transmem

93 herein disclose a computational study on the homo- and heterodimerization of isocyanides, in particul

94 To study the consequences of homo- and heterodimerization of wild-type and mutant PTE

95 The regulation of MST1/2 includes both homo- and heterodimerization, mediated by helical SARAH

96 GPCRs assemble into complexes, through both homo- and heterodimerization.

97 Although homo- and heterodimerizations of G protein-coupled recep

98 and EHD3 have 86% amino acid identity; they homo- and heterodimerize and partially co-localize to TR

99 NKD1 and NKD2 can homo- and heterodimerize through their ID domains.

100 Given that NAC53 and NAC78 homo- and heterodimerize, we propose that they work as a

101 re obtained via implicit solvent modeling of homo- and heterodimers and analysis of interactions in t

102 , we report that both ATase1 and ATase2 form homo- and heterodimers and associate with members of the

103 Cys mutants, which purified as a mixture of homo- and heterodimers at volumes consistent with a tetr

104 ists between constitutive and ligand-induced homo- and heterodimers capable of shaping transmembrane

105 and purified, the resulting acyl-CoA oxidase homo- and heterodimers displayed different side-chain le

106 tereocontrolled synthesis of ribonucleosidic homo- and heterodimers has been achieved from inexpensiv

107 These receptors form homo- and heterodimers in response to ligand with ErbB2

108 ata demonstrate for the first time that both homo- and heterodimers of ABCD1 and ABCD2 are functional

109 ically analyze dimerization of 18 TM helical homo- and heterodimers of different bitopic proteins, in

110 , we describe the synthesis of a full set of homo- and heterodimers of three intact structures of dif

111 These findings uncover a novel network of homo- and heterodimers of ZnTs with distinct subcellular

112 X-seq) on several floral MADS domain protein homo- and heterodimers to measure their DNA binding spec

113 cation of Intact Glycopeptides", noncovalent homo- and heterodimers were mis-identified as glycopepti

114 We report that 5-HT2 receptors can form homo- and heterodimers when expressed alone or co-expres

115 eta-oxidation cycles, form different protein homo- and heterodimers with distinct substrate preferenc

116 ar regions and promote formation of specific homo- and heterodimers with enhanced tyrosine kinase act

117 bZIP28 forms homo- and heterodimers with other bZIP TF family members

118 PCR dimerization, functional consequences of homo- and heterodimers, and approaches of medicinal chem

119 HDAC1 and -2 form homo- and heterodimers, and their activity is dependent

120 They form homo- and heterodimers, and then collaboratively regulat

121 ps between structure and function in the RTY homo- and heterodimers, and unveiled the likely structur

122 optosome mediates the formation of caspase-9 homo- and heterodimers, both of which are impacted by cl

123 pase-9-p35/p12 inhibited its ability to form homo- and heterodimers, but feedback cleavage by caspase

124 hing cellular responses to IL-17A and IL-17F homo- and heterodimers.

125 ed, thus demonstrating functionality of both homo- and heterodimers.

126 lize MICU1 dimers, allowing exchange between homo- and heterodimers.

127 mechanisms of binding and stripping for both homo- and heterodimers.

128 rikingly different reactivity of a series of homo- and heterodinuclear [(M(III) )(mu-O)2 (M(III) )'](

129 In this approach, unprotected homo- and heterodipeptides (including aromatic, aliphati

130 Homo- and heterodivalent crown-ammonium pseudorotaxanes

131 e thermal stability experiments conducted on homo- and heteroduplexes made of (S)-ZNA are described t

132 Homo- and heterofunctionalized glycoclusters with galact

133 ross sections, and composite structures with homo- and heterogeneous components.

134 s and enables a superior characterization of homo- and heterogenic systems.

135 evels in S-cells in multiple combinations of homo- and heterografts of gtr1 gtr2, biosynthetic null m

136 his study, we show how the interplay between homo- and heteroion pairing influences protein stability

137 sized a series of chlorophosphines utilizing homo- and heteroleptic (dianionic)guanidinates and have

138 Live FRET imaging suggested that both homo- and heteromeric AdipoR complexes dissociate in res

139 biogenesis of functionally diverse pools of homo- and heteromeric AMPAR tetramers.

140 e of PhTX-74 and related polyamine toxins at homo- and heteromeric AMPARs in the presence and absence

141 How cells regulate the formation of diverse homo- and heteromeric AMPARs is unknown.

142 C20, supporting the biochemical data showing homo- and heteromeric assembly of the CNGC20 and CNGC19

143 ology and membrane anchor domains and blocks homo- and heteromeric CerS2/6 complex formation and acti

144 f the immunocomplex, we show the presence of homo- and heteromeric complexes for human TPC1 and TPC2.

145 hich indicates that AdipoR1 and AdipoR2 form homo- and heteromeric complexes under resting conditions

146 therefore, on the steady-state proportion of homo- and heteromeric complexes.

147 ha1(Q-26'E)) enhances receptor activation in homo- and heteromeric glycine receptors.

148 ssay, called type-4 BRET, which detects both homo- and heteromeric interactions using induced multime

149 durations and reduced channel conductance in homo- and heteromeric receptors.

150 Homo- and heteromerization were confirmed by a FRET stud

151 rane spanning (7TM) receptors/GPCRs can form homo- and heteromers and initiate distinct signaling pat

152 the transitions between B4GALT1 and ST6GAL1 homo- and heteromers in the Golgi, and cooperative B4GAL

153 dings indicate that AdipoR1 and AdipoR2 form homo- and heteromers that present unique interaction beh

154 n the endoplasmic reticulum (ER) and to form homo- and heteromers.

155 xt of using a series of strongly oxo-coupled homo- and heterometallic poly(f-block) chains to better

156 romising features, the synthesis of targeted homo- and heterometallic titanium-organic frameworks ame

157 two-dimensional NMR approaches based on both homo- and heteronuclear couplings ((1)H-(1)H COSY; (1)H-

158 abolite content, leading to remarkably clean homo- and heteronuclear NMR spectra of the serum metabol

159 The relevant homo- and heteronuclear spin-spin couplings are reported

160 y transfer to characterize the energetics of homo- and heterooligomer interactions between the Vpu TM

161 on paramagnetic resonance (EPR) to probe the homo- and heterooligomeric interactions of reconstituted

162 6-Phosphofructokinases (Pfk) are homo- and heterooligomeric, allosteric enzymes that cata

163 of ARF and Aux/IAA proteins facilitate their homo- and heterooligomerization, the molecular basis for

164 GFP assays indicate that Arabidopsis SWEETs homo- and heterooligomerize.

165 ORMDL proteins formed homo- and heterooligomers and displayed similar patterns

166 h MDMX, the function and regulation of these homo- and heterooligomers in vivo remain incompletely un

167 these Delta proteins can bind to one another homo- and heterophilically, and to study the localisatio

168 Homo- and heteropolymeric tracts of A and T demarcate nu

169 epare multiple two-loop structures with both homo- and heterosequences.

170 Homo- and heterospectral correlation analysis are powerf

171 of the cooperative effect of substituents in homo- and heterosubstituted oligomers.

172 To determine the prevalence for human homo- and heterosubtypic antibody responses, we scrutini

173 responses that contribute to protection from homo- and heterosubtypic IAV infections.

174 de evidence that vaccinations stimulate both homo- and heterosubtypic immune responses in young and m

175 es and conferred complete protection against homo- and heterosubtypic lethal virus challenges.

176 emical systems, owing to its ability to form homo- and heteroternary complexes in aqueous media with

177 as a homotetramer channel, in astrocytes as homo- and heterotetramer channels together with KIR5.1.

178 dividual IP3R monomers are assembled to form homo- and heterotetrameric channels that mediate Ca(2+)

179 nonselective cation channels that form many homo- and heterotetrameric channels.

180 ing cellular homeostasis by the formation of homo- and heterotetrameric complexes.

181 nstrate that both transporters exist as both homo- and heterotetramers, with a predominance of homote

182 or modeling lies in capturing the panoply of homo- and heterotypic cellular interactions within the c

183 igomerized with comparable efficiency in all homo- and heterotypic combinations, but only the homotyp

184 ultidomain transmembrane proteins possessing homo- and heterotypic contact sites in their ectodomains

185 ue-ECM boundary, rather than by differential homo- and heterotypic energies of cell-cell interaction.

186 and, residues in the C'C" loop necessary for homo- and heterotypic interactions are dispensable for M

187 olos, Eos, and Pegasus, which engage in both homo- and heterotypic intrafamilial interactions to exer

188 9 system enables the generation of transient homo- and heterozygous deletion libraries and allows for

189 ntaining a diverse set of glycans, including homo- and mixed N-glycans (high-mannose, hybrid and comp

190 ur structure revision, but the structures of homo- and nor-plakotenin must also be revised.

191 Furthermore, a series of TPD homo- and pseudohomopolymers bearing various alkyl chain

192 with both MDM2 and MDMX by inhibitor-driven homo- and/or heterodimerization of MDM2 and MDMX protein

193 Nuclear receptors (NRs) form homo- and/or heterodimers as central scaffolds of multip

194 stress, MRs and GRs seem to bind to GREs as homo- and/or heterodimers in a gene-dependent manner.

195 Rs) associate in the plasma membrane to form homo- and/or heteromers.

196 arguments, the electron distributions in the HOMOs, and NBO/NRT analyses.

197 BTI units leads to polymers with a low-lying HOMOs ( approximately -5.6 eV).

198 hat the highest occupied molecular orbitals (HOMOs) are localized (24-99%) in all cruciforms, in cont

199 ory insertion barriers due to a lower-energy HOMO, as well as high C-O reductive elimination barriers

200 ssed in lung epithelial A549 cells, can form homo- as well as heteromers.

201 ar machine capable of sequence-specific beta-homo (beta(3)) peptide synthesis.

202 f indole highest occupied molecular orbital (HOMO) charge density toward the cation with a subsequent

203 us with derived morphology observed in later Homo, confirming that dentognathic departures from the a

204 cerns the fate of archaic forms of the genus Homo: did they go extinct without interbreeding with ana

205 r similarity and ability to form hetero (and homo) dimers, DDX5 and DDX17 are used by HIV in differen

206 Children less than 3 years old in Abu Homos, Egypt, had approximately five diarrheal episodes

207 range of highest occupied molecular orbital (HOMO) energies as determined by cyclovoltammetry.

208 orbates' highest occupied molecular orbital (HOMO) energies.

209 pshifted highest occupied molecular orbital (HOMO) energy level mainly due to the additional octyl on

210 ince the first discovery of Pithecanthropus (Homo) erectus by E.

211 y compresses polymer bandgaps and lowers the HOMOs--essential to maximize power conversion efficiency

212 Whereas a simple HOMO-->LUMO-type single substitution perfectly accounts

213 S(1) state of a molecule is dominated by the HOMO->LUMO excitation, a comparably simple but theoretic

214 e show that reduction in molar size in early Homo (H. habilis and H. rudolfensis) is explicable by ph

215 elated behavioural differences between early Homo (H. habilis and/or H. rudolfensis) and Homo erectus

216 that the highest occupied molecular orbital (HOMO) has mixed metal-ligand character rather than being

217 revealing that the lowering of the energy of HOMO (Highly Occupied Molecular Orbital) discourages the

218 genera Australopithecus, Kenyanthropus, and Homo; however, Theropithecus and Paranthropus have simil

219 highest (doubly) occupied molecular orbital (HOMO) in both axial and helical bicarbazole monoradicals

220 However, in species of Homo, including modern humans, there is a tight link bet

221 a deeper highest occupied molecular orbital (HOMO) level for obtaining polymer solar cells with a hig

222 xhibit a highest occupied molecular orbital (HOMO) level of -4.82 eV and a hole mobility up to 2.16x1

223 ring the highest occupied molecular orbital (HOMO) level of the nanofiber building blocks.

224 a higher highest occupied molecular orbital (HOMO) level, a lower lowest unoccupied molecular orbital

225 e of the highest occupied molecular orbital (HOMO) localized on the six-atom Sc(4)O(2) cluster.

226 d to the highest occupied molecular orbital (HOMO)-lowest unoccupied molecular orbital (LUMO) gap in

227 (159 of 225) are described by singly excited HOMO -> LUMO configurations, providing a rational for th

228 ral modifications could be used to alter the HOMO, LUMO, and band gap over a range of 1.0, 0.5, and 0

229 and electrochemical studies show that their HOMOs, LUMOs, and energy gaps can be easily modified or

230 ve of a strong dependence upon energy of the HOMO: measured rates of protonation vary over 6 orders o

231 donor molecules with relatively high energy HOMO, molecules with high HOMO-LUMO gaps and acceptor mo

232 cimens of Paranthropus, Australopithecus and Homo (n = 97), we find that the H. naledi premolars from

233 ween the highest occupied molecular orbital (HOMO) of N,N'-bis(1-naphthyl)N,N'-diphenyl-1,1'-biphenyl

234 ause the highest occupied molecular orbital (HOMO) of TCO is significantly higher in energy than the

235 l of the highest occupied molecular orbital (HOMO) of the considered arylogous ynolethers and ynamine

236 .e., the highest occupied molecular orbital (HOMO) or HOMO-n (n >/= 0) when the HOMO is not located o

237 bditis elegans PKD, DKF-2A, are exclusively (homo- or hetero-) dimers in cell extracts and intact cel

238 and PopD insert pores into membranes forming homo- or hetero-complexes of undetermined stoichiometry.

239 owth-factor ligands typically signal through homo- or hetero-dimeric cell surface receptors via Janus

240 at formation of one or more disulfide-linked homo- or hetero-dimeric proteins might signal photorecep

241 The coiled-coil motif that mediates homo- or hetero-dimerization of the bZIP proteins has be

242 a unique multimeric feature, forming either homo- or hetero-dimers, allowing the enzyme to use divis

243 (LRRC8) family members and contain LRRC8A in homo- or hetero-hexameric assemblies.

244 ose and can be linked to create single-chain homo- or hetero-ligands of defined stoichiometry.

245 ium binding C2A domain that mediates protein homo- or hetero-meric interactions.

246 odate a large variety of organic ligands and homo- or hetero-metallic clusters, which allows for extr

247 structure determination of membrane-embedded homo- or hetero-oligomeric Bcl-2 proteins via EPR.

248 oteins frequently assemble into higher order homo- or hetero-oligomers within their natural lipid env

249 t a large portion of nanoparticles will form homo- or heteroagglomerates when released into environme

250 background of SDE is a dynamic formation of homo- or heterochiral dimeric or oligomeric aggregates o

251 h it is well known that Ascl1 binds DNA as a homo- or heterodimer via its basic helix-loop-helix (bHL

252 here the hypothesis that ALX might exist as homo- or heterodimer with FPR1 or FPR3 (the two other fa

253 ch can be further exploited for a variety of homo- or heterodimeric receptors to achieve signaling, e

254 Here, we focus on antiparallel homo- or heterodimeric small multidrug resistance protei

255 inent in biology, and receptor dimerization (homo- or heterodimerization) is central to signal transd

256 eptor (TIR) domains of the receptors undergo homo- or heterodimerization.

257 may modulate cell survival and death through homo- or heterodimerization.

258 S proteins that are likely involved in their homo- or heterodimerization.

259 mice in which neither Notch1 nor Notch2 can homo- or heterodimerize, essential for cooperative bindi

260 ) and U1-70K revealed that U2AF(35) can form homo- or heterodimers and that U2AF(35) proteins can ass

261 However, certain covalent homo- or heterodimers eliminated twitching motility, sug

262 to one or more targets are co-synthesized as homo- or heterodimers or multimers via phosphodiester li

263 These receptors can function as homo- or heterodimers such as TR:9-cis retinoic acid rec

264 HLH122 and bHLH51 act sequentially as either homo- or heterodimers to choreograph tapetal development

265 ) signaling is affected by formation of GPCR homo- or heterodimers, but GPCR regulation by other cell

266 Furthermore, SGR1 and SGR2 formed homo- or heterodimers, strongly suggesting a role for SG

267 ut nearly 200 of these peptides are found as homo- or heterodimers.

268 regulate the preferential formation of Hax-1 homo- or heterodimers.

269 rs by expressing chimeric proteins mimicking homo- or heterodimers.

270 ADO can use a diiron cofactor (rather than a homo- or heterodinuclear cluster involving another trans

271 AMPARs are tetramers formed by homo- or heteromeric assembly of GluA1-4 subunits to pro

272 the transient aggregation/disaggregation of homo- or heteromeric building blocks.

273 from Xenopus oocytes expressing recombinant homo- or heteromeric combinations of GluA1, GluA2, and G

274 The switch between homo- or heteromeric DLK-1 complexes is influenced by Ca

275 Functional receptors are homo- or heteromeric tetramers with each subunit contrib

276 be subsequently trapped via coordination of homo- or heterometal adatoms, which may also play a role

277 ed PKD polypeptides may interact to generate homo- or heteromultimeric regulatory complexes.

278 logical signals and systems and are found in homo- or heteromultimerization of signaling molecules as

279 exes are used as building blocks to generate homo- or heteromultimetallic dinitrogen species, which a

280 ol-mediated cognitive impairment arises from homo- or heterooligomerization between the GPCRs cannabi

281 of the nature of the spacer used or whether homo- or heteroprotein dimers are targeted.

282 exogenously expressed human Kv7.4 and Kv7.5 homo- or heterotetrameric channels in A7r5 cells.

283 Kv7 (KCNQ) channels, formed as homo- or heterotetramers of Kv7.4 and Kv7.5 alpha-subuni

284 Homo- or heterozygosity at Ars1127354 or Crs7270101 , en

285 Homo- or heterozygous presence of the frequent [C] allel

286 nditions with various organic substrates and homo- or mixed-sequenced ODNs.

287 ins and suggest that substrate dimerization (homo- or possibly heterodimerization) might represent a

288 to Homo erectus These crania also show that Homo, Paranthropus, and Australopithecus were contempora

289 tors, namely HOMO energy of the catalyst ( E(HOMO)), percent buried volume ( V(bur)%), and distortion

290 Instead, an excited state formed by a Ph-NN (HOMO) --> Ph-NN (LUMO) one-electron promotion configurat

291 d beta-activation of carbonyl compounds, via HOMO, SOMO or LUMO activation pathways.

292 y higher highest occupied molecular orbital (HOMO) than the host polymer.

293 nfluence: bulky substituents destabilize the HOMO, thereby increasing the rate of protonation.

294 k Fermi level pinning (UPS revealed E(F) - E(HOMO) varied only weakly with Phi), but R(0) varies stro

295 ples the highest occupied molecular orbital (HOMO, which is localized on the carboxylate group) from

296 d is the highest occupied molecular orbital (HOMO) with a "bent" geometry.

297 via the highest occupied molecular orbital (HOMO) with a rectification ratio R = 99, but junctions w

298 uitable highest occupied molecular orbitals (HOMO) with respect to the valence band level of the pero

299 volving hole transport through the molecular HOMO, with a decay constant beta = 3.4 +/- 0.1 nm(-1) an

300 s to the highest occupied molecular orbital (HOMO)-with a Ge-centred lone pair as the HOMO-1.